IDEAS home Printed from https://ideas.repec.org/a/gam/jijerp/v17y2020i21p8048-d438473.html
   My bibliography  Save this article

Patient and Public Involvement in Sexual and Reproductive Health: Time to Properly Integrate Citizen’s Input into Science

Author

Listed:
  • Miguel García-Martín

    (Department of Preventive Medicine and Public Health, Faculty of Medicine, University of Granada, 18016 Granada, Spain
    Consortium for Biomedical Research in Epidemiology and Public Health (CIBERESP), 28029 Madrid, Spain
    Instituto de Investigación Biosanitaria (ibs.Granada), 18014 Granada, Spain)

  • Carmen Amezcua-Prieto

    (Department of Preventive Medicine and Public Health, Faculty of Medicine, University of Granada, 18016 Granada, Spain
    Consortium for Biomedical Research in Epidemiology and Public Health (CIBERESP), 28029 Madrid, Spain
    Instituto de Investigación Biosanitaria (ibs.Granada), 18014 Granada, Spain)

  • Bassel H Al Wattar

    (Reproductive Medicine Unit, Institute for Women’s Health, University College London Hospitals, London WC1E 6BT, UK
    Warwick Medical School, University of Warwick, Coventry CV4 7 AL, UK)

  • Jan Stener Jørgensen

    (Department of Obstetrics and Gynaecology CIMT-Centre for Innovative Medical Technologies Odense University Hospital, 5000 Odense C, Denmark)

  • Aurora Bueno-Cavanillas

    (Department of Preventive Medicine and Public Health, Faculty of Medicine, University of Granada, 18016 Granada, Spain
    Consortium for Biomedical Research in Epidemiology and Public Health (CIBERESP), 28029 Madrid, Spain
    Instituto de Investigación Biosanitaria (ibs.Granada), 18014 Granada, Spain)

  • Khalid Saeed Khan

    (Department of Preventive Medicine and Public Health, Faculty of Medicine, University of Granada, 18016 Granada, Spain
    Consortium for Biomedical Research in Epidemiology and Public Health (CIBERESP), 28029 Madrid, Spain)

Abstract

Evidence-based sexual and reproductive health is a global endeavor without borders. Inter-sectorial collaboration is essential for identifying and addressing gaps in evidence. Health research funders and regulators are promoting patient and public involvement in research, but there is a lack of quality tools for involving patients. Partnerships with patients are necessary to produce and promote robust, relevant and timely research. Without the active participation of women as stakeholders, not just as research subjects, the societal benefits of research cannot be realized. Creating and developing platforms and opportunities for public involvement in sexual and reproductive health research should be a key international objective. Cooperation between healthcare professionals, academic institutions and the community is essential to promote quality research and significant developments in women’s health. This cooperation will be improved when involvement of citizens in the research process becomes standard.

Suggested Citation

  • Miguel García-Martín & Carmen Amezcua-Prieto & Bassel H Al Wattar & Jan Stener Jørgensen & Aurora Bueno-Cavanillas & Khalid Saeed Khan, 2020. "Patient and Public Involvement in Sexual and Reproductive Health: Time to Properly Integrate Citizen’s Input into Science," IJERPH, MDPI, vol. 17(21), pages 1-12, October.
  • Handle: RePEc:gam:jijerp:v:17:y:2020:i:21:p:8048-:d:438473
    as

    Download full text from publisher

    File URL: https://www.mdpi.com/1660-4601/17/21/8048/pdf
    Download Restriction: no

    File URL: https://www.mdpi.com/1660-4601/17/21/8048/
    Download Restriction: no
    ---><---

    References listed on IDEAS

    as
    1. Caron-Flinterman, J. Francisca & Broerse, Jacqueline E.W. & Bunders, Joske F.G., 2005. "The experiential knowledge of patients: a new resource for biomedical research?," Social Science & Medicine, Elsevier, vol. 60(11), pages 2575-2584, June.
    2. Jo Brett & Sophie Staniszewska & Carole Mockford & Sandra Herron-Marx & John Hughes & Colin Tysall & Rashida Suleman, 2014. "A Systematic Review of the Impact of Patient and Public Involvement on Service Users, Researchers and Communities," The Patient: Patient-Centered Outcomes Research, Springer;International Academy of Health Preference Research, vol. 7(4), pages 387-395, December.
    Full references (including those not matched with items on IDEAS)

    Citations

    Citations are extracted by the CitEc Project, subscribe to its RSS feed for this item.
    as


    Cited by:

    1. Amira Bouzalmate-Hajjaj & Paloma Massó Guijarro & Khalid Saeed Khan & Aurora Bueno-Cavanillas & Naomi Cano-Ibáñez, 2022. "Benefits of Participation in Clinical Trials: An Umbrella Review," IJERPH, MDPI, vol. 19(22), pages 1-11, November.
    2. Juan Miguel Martínez-Galiano & Miguel Delgado-Rodríguez, 2021. "The Relegated Goal of Health Institutions: Sexual and Reproductive Health," IJERPH, MDPI, vol. 18(4), pages 1-4, February.

    Most related items

    These are the items that most often cite the same works as this one and are cited by the same works as this one.
    1. Ziewitz, Malte, 2017. "Experience in action: Moderating care in web-based patient feedback," Social Science & Medicine, Elsevier, vol. 175(C), pages 99-108.
    2. Stockl, Andrea, 2007. "Complex syndromes, ambivalent diagnosis, and existential uncertainty: The case of Systemic Lupus Erythematosus (SLE)," Social Science & Medicine, Elsevier, vol. 65(7), pages 1549-1559, October.
    3. Kathryn Oliver & Annette Boaz, 2019. "Transforming evidence for policy and practice: creating space for new conversations," Palgrave Communications, Palgrave Macmillan, vol. 5(1), pages 1-10, December.
    4. Mathieu Ahouah & Monique Rothan-Tondeur, 2019. "End-Users and Caregivers’ Involvement in Health Interventional Research Carried Out in Geriatric Facilities: A Systematic Review," IJERPH, MDPI, vol. 16(16), pages 1-14, August.
    5. Alexandre Trigo, 2016. "Innovation in the Era of Experience: The Changing Role of Users in Healthcare Innovation," Journal of Entrepreneurship, Management and Innovation, Fundacja Upowszechniająca Wiedzę i Naukę "Cognitione", vol. 12(2), pages 29-51.
    6. Allen, Dawn & Wainwright, Megan & Hutchinson, Thomas, 2011. "'Non-compliance' as illness management: Hemodialysis patients' descriptions of adversarial patient-clinician interactions," Social Science & Medicine, Elsevier, vol. 73(1), pages 129-134, July.
    7. Elberse, Janneke Elisabeth & Pittens, Carina Anna Cornelia Maria & de Cock Buning, Tjard & Broerse, Jacqueline Elisabeth Willy, 2012. "Patient involvement in a scientific advisory process: Setting the research agenda for medical products," Health Policy, Elsevier, vol. 107(2), pages 231-242.
    8. Luisi, Daniela & Hämel, Kerstin, 2021. "Community participation and empowerment in primary health care in Emilia-Romagna: A document analysis study," Health Policy, Elsevier, vol. 125(2), pages 177-184.
    9. Melvyn W.B. Zhang & Jiangbo Ying, 2019. "Incorporating Participatory Action Research in Attention Bias Modification Interventions for Addictive Disorders: Perspectives," IJERPH, MDPI, vol. 16(5), pages 1-11, March.
    10. Modigh, Anton & Sampaio, Filipa & Moberg, Linda & Fredriksson, Mio, 2021. "The impact of patient and public involvement in health research versus healthcare: A scoping review of reviews," Health Policy, Elsevier, vol. 125(9), pages 1208-1221.
    11. Rojatz, Daniela & Forster, Rudolf, 2017. "Self-help organisations as patient representatives in health care and policy decision-making," Health Policy, Elsevier, vol. 121(10), pages 1047-1052.
    12. Matias Ramirez & Javier Hernando Garcia Estevez & Oscar Yandy Romero Goyeneche & Claudia E Obando Rodriguez, 2020. "Fostering place-based coalitions between social movements and science for sustainable urban environments: A case of embedded agency," Environment and Planning C, , vol. 38(7-8), pages 1386-1411, November.
    13. Beck, Susanne & Brasseur, Tiare-Maria & Poetz, Marion & Sauermann, Henry, 2022. "Crowdsourcing research questions in science," Research Policy, Elsevier, vol. 51(4).
    14. Papoulias, Stan (Constantina) & Callard, Felicity, 2022. "Material and epistemic precarity: It's time to talk about labour exploitation in mental health research," Social Science & Medicine, Elsevier, vol. 306(C).
    15. Barbara Groot & Annyk Haveman & Mireille Buree & Ruud van Zuijlen & Juliette van Zuijlen & Tineke Abma, 2022. "What Patients Prioritize for Research to Improve Their Lives and How Their Priorities Get Dismissed again," IJERPH, MDPI, vol. 19(4), pages 1-15, February.
    16. Andrea Fogarty & Zachary Steel & Philip B. Ward & Katherine M. Boydell & Grace McKeon & Simon Rosenbaum, 2021. "Trauma and Mental Health Awareness in Emergency Service Workers: A Qualitative Evaluation of the Behind the Seen Education Workshops," IJERPH, MDPI, vol. 18(9), pages 1-16, April.
    17. Simone Harmsen & Carina A C M Pittens & Eva Vroonland & Annemiek J M L van Rensen & Jacqueline E W Broerse, 2022. "Supporting health researchers to realize meaningful patient involvement in research: Exploring researchers’ experiences and needs [New Requirements for Patient and Public Involvement Statements in ," Science and Public Policy, Oxford University Press, vol. 49(5), pages 751-764.
    18. Deml, Michael J. & Notter, Julia & Kliem, Paulina & Buhl, Andrea & Huber, Benedikt M. & Pfeiffer, Constanze & Burton-Jeangros, Claudine & Tarr, Philip E., 2019. "“We treat humans, not herds!”: A qualitative study of complementary and alternative medicine (CAM) providers’ individualized approaches to vaccination in Switzerland," Social Science & Medicine, Elsevier, vol. 240(C).
    19. Lehoux, Pascale & Poland, Blake & Daudelin, Genevieve, 2006. "Focus group research and "the patient's view"," Social Science & Medicine, Elsevier, vol. 63(8), pages 2091-2104, October.
    20. Goven, Joanna, 2008. "Assessing genetic testing: Who are the "lay experts"?," Health Policy, Elsevier, vol. 85(1), pages 1-18, January.

    Corrections

    All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:gam:jijerp:v:17:y:2020:i:21:p:8048-:d:438473. See general information about how to correct material in RePEc.

    If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.

    If CitEc recognized a bibliographic reference but did not link an item in RePEc to it, you can help with this form .

    If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.

    For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: MDPI Indexing Manager (email available below). General contact details of provider: https://www.mdpi.com .

    Please note that corrections may take a couple of weeks to filter through the various RePEc services.

    IDEAS is a RePEc service. RePEc uses bibliographic data supplied by the respective publishers.